Adrenocortical carcinoma (ACC) outcomes: What to expect?

Posted by annern @annern, Jan 12, 2025

I (F 67) was diagnosed with adrenal cortical carcinoma stage 2, Non secreting tumor in September 2024. Treatment of surgical removal, 25 days of radiation and now Chemotherapy with Mitotane (Lysodrin). I am looking for people with this diagnosis to compare side effects. I’m also on Hydrocortisone replacement. If anyone is further down the road than I am, please let me know how you are doing!

Interested in more discussions like this? Go to the Neuroendocrine Tumors (NETs) Support Group.

Profile picture for pbouey @pbouey

Hi, I am a 70 year old woman who had an adrenal tumor removed recently, and was informed I have ACC and the tumor, although removed, was very aggressive. I am to start the 2 years of Mitatone and am unsure of how this therapy will affect my lifestyle. I just retired and have 7 little grandchildren with whom I have been very involved, but from what I read the drug will compromise me significantly. Looking for comrades who are in this situation! Pamela

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@pbouey Hi and welcome to Mayo Connect. I don't know much about Adrenocortical Carcinoma nor Mitotane. Here are links from Mayo's website with information on ACC and Mitotane.
https://www.mayoclinic.org/diseases-conditions/adrenal-cancer/symptoms-causes/syc-20351026
https://www.mayoclinic.org/drugs-supplements/mitotane-oral-route/description/drg-20064841
This thread has some good input from others with ACC. Did you find anything helpful?

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Profile picture for Turkey, Volunteer Mentor @tomrennie

@pbouey Hi and welcome to Mayo Connect. I don't know much about Adrenocortical Carcinoma nor Mitotane. Here are links from Mayo's website with information on ACC and Mitotane.
https://www.mayoclinic.org/diseases-conditions/adrenal-cancer/symptoms-causes/syc-20351026
https://www.mayoclinic.org/drugs-supplements/mitotane-oral-route/description/drg-20064841
This thread has some good input from others with ACC. Did you find anything helpful?

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Thank you so much, I am just learning myself. This is such a rare cancer, finding information is sort of hard. Never thought I would be a cancer patient, but I guess everyone says that!

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Profile picture for pbouey @pbouey

Thank you so much, I am just learning myself. This is such a rare cancer, finding information is sort of hard. Never thought I would be a cancer patient, but I guess everyone says that!

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@pbouey You are right. No one ever thinks that they would be a cancer patient. Where have you been looking for information?

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Profile picture for Turkey, Volunteer Mentor @tomrennie

@pbouey You are right. No one ever thinks that they would be a cancer patient. Where have you been looking for information?

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@tomrennie
I have been looking all over the internet, plus I have a close friend who is a UCSF internal med physician who is watching all of this. The Mitatone phase sounds tricky and kind of horrible, but it might decrease the chances of recurrence.

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Profile picture for pbouey @pbouey

@tomrennie
I have been looking all over the internet, plus I have a close friend who is a UCSF internal med physician who is watching all of this. The Mitatone phase sounds tricky and kind of horrible, but it might decrease the chances of recurrence.

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@pbouey I know it is hard to find ACC information. I just want to caution you to be selective on where you get your information. I have learned that unless the information is coming from a reputable resource, it may not be correct.
I found another discussion on ACC on connect. I hope that you find it helpful.
https://connect.mayoclinic.org/discussion/adrenal-cancer/

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Hi All,

I am a 59 year old woman who was diagnosed with ACC in May. I had a very large tumor fully removed but had some significant complications after surgery. Once I recovered I did 25 days of radiation and I am currently waiting to start Mitotane because my liver was adversely affected by the radiation and some of my enzymes are high. Did anyone else have issues with their liver enzymes after radiation? Just curious. Also I am technically considered stage 3 because of the size of my tumor but no evidence that it has spread anywhere else in my body. I would.love to be able to connect with others who are dealing with this disease. Thank you.

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